Western Psychiatric Institute and Clinic, Pittsburgh.
Bloorview Research Institute, Holland Bloorview Kids Rehabilitation Hospital, University of Toronto, Toronto, Canada.
J Am Acad Child Adolesc Psychiatry. 2017 Oct;56(10):849-856.e6. doi: 10.1016/j.jaac.2017.07.790. Epub 2017 Aug 19.
A previous study reported on a 16-week placebo-controlled, randomized clinical trial (RCT) of metformin for weight stabilization in 61 children and adolescents 6 to 17 years old with autism spectrum disorder who were prescribed atypical antipsychotics. The present study describes the results of a 16-week open-label extension.
Fifty-two participants from the acute trial (85%) entered the extension; 22 had been on metformin during the initial RCT and 30 had been on placebo. Participants were re-titrated to 500 mg twice a day (6- to 9-year-olds) or 850 mg twice a day (10- to 17-year-olds) during the open-label extension. Primary outcome measure was change in body mass index (BMI) z-score after 16 weeks; secondary outcomes were change in additional body composition and metabolic parameters.
After 16 weeks of open-label treatment, participants initially taking placebo during the RCT had lower BMI z-scores (mean 16-week change -0.10, p = .004). Statistically significant improvements also were noted in secondary body composition measures (weight z-score and BMI and weight percentile) but not in metabolic variables. Participants who initially had been taking metformin during the 16-week RCT maintained prior decreases in BMI z-scores but did not have additional weight loss. Three participants discontinued treatment because of an adverse event. No significant changes were noted on metabolic measures, although the decrease in hemoglobin A was large (∼1 mmol) and consistent across the acute and open-label phases.
Metformin can be effective for decreasing weight gain associated with atypical antipsychotic use and maintaining prior improvement in children and adolescents with autism spectrum disorder. Clinical trial registration information-Treatment of Overweight Induced by Antipsychotic Medication in Young People With Autism Spectrum Disorders (ASD); http://clinicaltrials.gov/; NCT01825798.
先前的一项研究报告了一项为期 16 周的安慰剂对照、随机临床试验(RCT)的结果,该研究纳入了 61 名 6 至 17 岁的自闭症谱系障碍儿童和青少年,他们正在服用非典型抗精神病药物,该 RCT 旨在评估二甲双胍对体重稳定的作用。本研究描述了 16 周开放标签扩展试验的结果。
急性试验中的 52 名参与者(85%)进入了扩展试验;其中 22 名参与者在初始 RCT 期间服用二甲双胍,30 名参与者服用安慰剂。在开放标签扩展期间,参与者重新滴定剂量至每天两次 500mg(6 至 9 岁)或每天两次 850mg(10 至 17 岁)。主要结局指标为 16 周后体重指数(BMI)z 评分的变化;次要结局指标为其他身体成分和代谢参数的变化。
在 16 周的开放标签治疗后,在 RCT 期间最初服用安慰剂的参与者 BMI z 评分较低(平均 16 周变化-0.10,p=0.004)。次要身体成分指标(体重 z 评分和 BMI 及体重百分位)也有显著改善,但代谢变量无显著改善。在 RCT 的 16 周期间最初服用二甲双胍的参与者维持了先前 BMI z 评分的降低,但没有额外的体重减轻。3 名参与者因不良事件停止治疗。代谢指标无显著变化,但血红蛋白 A 的下降较大(约 1mmol),且在急性和开放标签阶段一致。
二甲双胍可有效减少与非典型抗精神病药物相关的体重增加,并维持自闭症谱系障碍儿童和青少年先前的体重改善。临床试验注册信息-治疗自闭症谱系障碍青少年因抗精神病药物引起的超重(ASD);http://clinicaltrials.gov/;NCT01825798。